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首页> 外文期刊>Applied and Environmental Microbiology >Isolation of Bifidobacteria from Breast Milk and Assessment of the Bifidobacterial Population by PCR-Denaturing Gradient Gel Electrophoresis and Quantitative Real-Time PCR
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Isolation of Bifidobacteria from Breast Milk and Assessment of the Bifidobacterial Population by PCR-Denaturing Gradient Gel Electrophoresis and Quantitative Real-Time PCR

机译:从母乳中分离双歧杆菌并通过PCR-变性梯度凝胶电泳和定量实时PCR评估双歧杆菌的数量

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摘要

The objective of this work was to elucidate if breast milk contains bifidobacteria and whether they can be transmitted to the infant gut through breastfeeding. Twenty-three women and their respective infants provided samples of breast milk and feces, respectively, at days 4 to 7 after birth. Gram-positive and catalase-negative isolates from specific media with typical bifidobacterial shapes were identified to the genus level by F6PPK (fructose-6-phosphate phosphoketolase) assays and to the species level by 16S rRNA gene sequencing. Bifidobacterial communities in breast milk were assessed by PCR-denaturing gradient gel electrophoresis (PCR-DGGE), and their levels were estimated by quantitative real-time PCR (qRTi-PCR). Bifidobacteria were present in 8 milk samples and 21 fecal samples. Bifidobacterium breve, B. adolescentis, and B. bifidum were isolated from milk samples, while infant feces also contained B. longum and B. pseudocatenulatum. PCR-DGGE revealed the presence of one to four dominant bifidobacterial bands in 22 milk samples. Sequences with similarities above 98% were identified as Bifidobacterium breve, B. adolescentis, B. longum, B. bifidum, and B. dentium. Bifidobacterial DNA was detected by qRTi-PCR in the same 22 milk samples at a range between 40 and 10,000 16S rRNA gene copies per ml. In conclusion, human milk seems to be a source of living bifidobacteria for the infant gut.
机译:这项工作的目的是阐明母乳中是否含有双歧杆菌,以及它们是否可以通过母乳喂养传染给婴儿肠道。 23名妇女及其各自的婴儿在出生后第4至7天分别提供了母乳和粪便的样本。通过F6PPK(果糖6磷酸磷酸酮醇酶)测定,从具有典型双歧杆菌形状的特定培养基中分离出革兰氏阳性和过氧化氢酶阴性分离株,并通过16S rRNA基因测序鉴定出种属水平。母乳中的双歧杆菌群落通过PCR变性梯度凝胶电泳(PCR-DGGE)进行评估,其水平通过实时定量PCR(qRTi-PCR)进行评估。双歧杆菌存在于8个牛奶样品和21个粪便样品中。从牛奶样品中分离了短双歧杆菌,青春双歧杆菌和双歧双歧杆菌,而婴儿粪便中还含有长双歧杆菌和假双歧杆菌。 PCR-DGGE揭示了22个牛奶样品中存在1-4个主要双歧杆菌带。相似性高于98%的序列被鉴定为短双歧杆菌,青春双歧杆菌,长双歧杆菌,双歧双歧杆菌和齿状双歧杆菌。通过qRTi-PCR在相同的22个牛奶样品中检测到双歧杆菌DNA,其范围介于每毫升40到10,000个16S rRNA基因拷贝之间。总之,母乳似乎是婴儿肠道中活的双歧杆菌的来源。

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